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JPH0250817A - Method and device for manufacturing plastic continuum - Google Patents

Method and device for manufacturing plastic continuum

Info

Publication number
JPH0250817A
JPH0250817A JP1142019A JP14201989A JPH0250817A JP H0250817 A JPH0250817 A JP H0250817A JP 1142019 A JP1142019 A JP 1142019A JP 14201989 A JP14201989 A JP 14201989A JP H0250817 A JPH0250817 A JP H0250817A
Authority
JP
Japan
Prior art keywords
plastic
roll
temperature
stretching
mol
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP1142019A
Other languages
Japanese (ja)
Other versions
JP2675140B2 (en
Inventor
Zaheer Bashir
ザエール・バッシャー
Cornelis Wilhelmus M Bastiaansen
コーネリス・ウィルヘルムス・マリア・バスティアンセン
Henricus Eduard Hubertus Meijer
ヘンリカス・エドゥアルド・ヒューバータス・メイヤー
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Stamicarbon BV
Original Assignee
Stamicarbon BV
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Stamicarbon BV filed Critical Stamicarbon BV
Publication of JPH0250817A publication Critical patent/JPH0250817A/en
Application granted granted Critical
Publication of JP2675140B2 publication Critical patent/JP2675140B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C55/00Shaping by stretching, e.g. drawing through a die; Apparatus therefor
    • B29C55/30Drawing through a die
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J5/00Manufacture of articles or shaped materials containing macromolecular substances
    • C08J5/18Manufacture of films or sheets
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C55/00Shaping by stretching, e.g. drawing through a die; Apparatus therefor
    • B29C55/005Shaping by stretching, e.g. drawing through a die; Apparatus therefor characterised by the choice of materials
    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01FCHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F6/00Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
    • D01F6/02Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D01F6/04Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds from polyolefins
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29KINDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
    • B29K2023/00Use of polyalkenes or derivatives thereof as moulding material
    • B29K2023/04Polymers of ethylene
    • B29K2023/06PE, i.e. polyethylene
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2323/00Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers
    • C08J2323/02Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers not modified by chemical after treatment
    • C08J2323/04Homopolymers or copolymers of ethene

Landscapes

  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Manufacturing & Machinery (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Mechanical Engineering (AREA)
  • Health & Medical Sciences (AREA)
  • Textile Engineering (AREA)
  • Materials Engineering (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Shaping By String And By Release Of Stress In Plastics And The Like (AREA)
  • Yarns And Mechanical Finishing Of Yarns Or Ropes (AREA)
  • Artificial Filaments (AREA)
  • Moulding By Coating Moulds (AREA)

Abstract

PURPOSE: To manufacture a tape and a film by converting a molten plastic having a relatively high molecular weight to a continuous object, and orienting the object while applying a stress at a specific temperature and a specific orienting speed to quench the object. CONSTITUTION: The plastic is formed of a polyethylene having 400000 to 1500000 G/mol, preferably 500000 to 1200000 G/mol or further preferably 800000 to 1000000 Mw. An extruded material from an extruder 1 is supplied to a cooler 2, and cooled to a melting temperature or lower. The cooled and unoriented extruded material is supplied to a supply roll. Supply rolls have only a roll 4 of a heating roll, heated to 5 to 10 deg.C lower than the melting point of the plastic, then continuously drawn via a furnace 6 by a take-off roll 5. The furnace heats the extruded material to 130 to 160 deg.C. The oriented material is quenched in a stress state between the furnace 6 and the take-off rolls 5, 7. Its orienting speed is 0.1 to 10 sec<-1> or preferably 0.5 to 5 sec<-1> .

Description

【発明の詳細な説明】 発明の分野 本発明はシシカバブ(shish kebab)形態を
有するプラスチック連続体の製造方法および装置に関す
る。
DETAILED DESCRIPTION OF THE INVENTION Field of the Invention The present invention relates to a method and apparatus for manufacturing plastic continuous bodies having a shish kebab morphology.

発明の背景 シシカバブ形態を有するフィラメントのようなプラスチ
ック連続体は欧州特許公開明細書EPA−151343
号により公知である。該連続体の形態は、ダイアプロー
チ内でポリオレフィンが自然に凝固する温度より数℃高
い温度を与えて、3X105〜10°g1モルの重量平
均分子量を有するポリオレフィンを押し出すことにより
得られる。
BACKGROUND OF THE INVENTION A filament-like plastic continuum having a shish kebab morphology is disclosed in European Patent Publication No. EPA-151343.
It is known by the number. The continuum morphology is obtained by extruding a polyolefin having a weight average molecular weight of 3×10 5 to 10° g 1 mol in a die approach, applying a temperature several degrees Celsius above the temperature at which the polyolefin spontaneously solidifies.

公知の方法の欠点は、ダイアブローチ内の温度を要求限
界内に保持することが難しく、実際に製造できる連続体
の製造速度がかなり遅いことである。また、その方法は
フィルムの製造にあまり適さない。
A disadvantage of the known method is that it is difficult to maintain the temperature within the diamond broach within the required limits, and the production rate of the continuous bodies that can be produced in practice is rather slow. Also, the method is not well suited for film production.

発明の開示 本発明の目的は前記欠点がなく、さらにテープおよびフ
ィルムの製造に適した連続体の製造方法および装置を提
供することである。これは、比較的高い重量平均分子量
(MW)を有する特定の種類の溶融体のプラスチックを
連続品に変換し、この連続品を未配向プラスチックの溶
融温度(Tm)と、より高温度(Tc)の間の温度で延
伸し、延伸速度が、通常の条件下での鎖状分子のりラク
ゼーションの速度より速い速度(Ve)と、それより高
いが、溶融体が通常の条件下で弾性挙動を示し始める程
は速くない速度の間にあって、応力を加えながら延伸さ
れた製品を連続体に急冷することにより実施される。
DISCLOSURE OF THE INVENTION It is an object of the present invention to provide a method and apparatus for the production of continuous bodies which do not have the above-mentioned disadvantages and which are furthermore suitable for the production of tapes and films. This converts certain types of melt plastics with relatively high weight-average molecular weights (MW) into a continuous article that has a melting temperature (Tm) of unoriented plastics and a higher temperature (Tc). If the stretching speed is higher than the rate of relaxation of the chain molecules under normal conditions (Ve), and the melt exhibits elastic behavior under normal conditions, It is carried out by quenching the stretched product into a continuous body while applying stress at a speed that is not fast enough to begin to show.

欧州特許公開明細書EP−A151343号には、ンン
カバブ形態が意味すること、および高強度を得るために
どのような条件が要求されるかについて広範に記載され
ている。さらにエルセビーア・アプライド・サイエンス
(Elsevier AppliedScience)
、ロンドンおよびニコーヨーク(Londonand 
Ne’w York)、1987により刊行されたアイ
・エム・ワード(1,M、Ward)により著述された
書籍「配向されたポリマー−1の開発」により引用でき
る。
European Patent Publication No. EP-A151343 describes extensively what is meant by nunkabab morphology and what conditions are required to obtain high strength. Additionally, Elsevier Applied Science
, London and Nico York
New York), 1987.

シシカバブ形態は、鎖に沿って存在しかつ屈曲分子鎖の
板状結晶から構成される[カバブ(kababs)Jと
呼ばれる全面成長(overgrowth)を有する[
シシ(shisi)Jと呼ばれる幾つかの伸長されたポ
リマー分子から構成されるコアによって特徴ずけられる
Shish kebab morphology exists along the chain and is composed of plate-shaped crystals of bent molecular chains [with overgrowth called kababs J]
It is characterized by a core composed of several elongated polymer molecules called shisi J.

[ラメラ(lamel 1ae)Jとも呼ばれる板状結
晶はコアを包囲し、該コアに関して角を成して配置され
ている。成形体において、該コアは互いに平行でかつ密
接しているため、片方のコアのラメラは他方のコアのラ
メラと重なっている。
[Plate crystals, also called lamellae J, surround the core and are arranged at angles with respect to the core. In the molded article, the cores are parallel and close to each other, so that the lamellae of one core overlap the lamellae of the other core.

もし溶融体の温度(Tc)が高くなりすぎると、未配向
分子鎖の溶融体から形成できる溶融体のシシカバブは延
伸工程の間に消失する。この温度は欧州特許公開明細書
EP=A−151343号により公知の成形品の溶融曲
線により、各ポリマーについて決定した。レプリカを用
いての電子顕微鏡による組織検査も好適な方法である。
If the melt temperature (Tc) becomes too high, the melt shish kebab that can be formed from the melt of unoriented molecular chains disappears during the drawing process. This temperature was determined for each polymer by means of the molding melting curve known from European Patent Application EP=A-151343. Tissue examination using an electron microscope using a replica is also a suitable method.

延伸温度は、このようにして判明した温度Tcを越える
べきではない。
The stretching temperature should not exceed the temperature Tc found in this way.

延伸速度にもは特別の注意を払う必要がある。Special attention should also be paid to the drawing speed.

ここで、延伸速度とは延伸比(ラムダ)を、延伸を行う
のに必要な時間(秒)で除したちである。ここで、延伸
速度(ラムダ)とは比L / L o (L oは初期
の長さ、■、は延伸後の長さ)である。延伸の間に2つ
の相反する現象が生じる。分子鎖は延伸力の影響下で伸
長されるため、延伸力の方向に平行に配列され、一方、
この現象は、該分子鎖をコイル状の不規則な状態に戻す
傾向にあるいわゆるリラクゼーション(relaxat
ion)により平衡する。該リラクゼーションはある速
度で進行するため、延伸速度はりラクゼーション速度よ
りも速くなければならない。これらの速度があるがまま
に互いに相殺する点および対応する延伸速度は経験的に
容易に決定できる:すなわち、低いMwを有するポリマ
ーについては固体のほうが液体よりも速く、それは高い
Mwを存するポリマーよりも速い。
Here, the stretching speed is the stretching ratio (lambda) divided by the time (seconds) required for stretching. Here, the stretching speed (lambda) is the ratio L/Lo (Lo is the initial length, ■ is the length after stretching). Two contradictory phenomena occur during stretching. As the molecular chains are stretched under the influence of the stretching force, they are aligned parallel to the direction of the stretching force;
This phenomenon is caused by the so-called relaxation, which tends to return the molecular chains to a coiled, disordered state.
ion). Since the relaxation proceeds at a certain speed, the stretching speed must be faster than the relaxation speed. The point at which these speeds cancel each other out as they are and the corresponding drawing speeds can be easily determined empirically: i.e., for polymers with low Mw, the solid is faster than the liquid; It's also fast.

延伸速度はあまり速すぎてはいけない。なぜならば、そ
うでないと溶融体は弾性的に反応し、切断するからであ
る。かくして、延伸速度は経験的に容易に決定できる。
The stretching speed should not be too high. This is because otherwise the melt would react elastically and break. Thus, the drawing speed can be easily determined empirically.

通常より高いEモジコラスおよび引張強度を達成するた
め、重量平均分子量MWは適当な限界内で選択されるべ
きである。Mwか小さずぎると、溶融体中でシンカバブ
形態が全く形成しないか、あるいは、ノンとカバブの比
が小さずぎるかまたはコアが離れすぎるシンカバブ形態
が形成されるため、ラメラは互いに重ならない。逆にM
wが大きすぎると、処理中、例えば押出機に問題が生じ
る。ここで当業者らは経験的な返りを用いる。
In order to achieve higher than usual E modicolus and tensile strength, the weight average molecular weight MW should be selected within appropriate limits. If Mw is too small, the lamellae do not overlap each other because either no shin-kebab morphology is formed in the melt, or because the non-to-kabab ratio is too small or the cores are too far apart. On the contrary, M
If w is too large, problems will occur during processing, for example in an extruder. Here, those skilled in the art use empirical advice.

技術的な見地からすると、広範な分子量分布を有するポ
リマーを用いると、ワラクゼーンヨン速度ど延伸速度が
互いに相殺する機会が多くなる。
From a technical standpoint, using polymers with a broad molecular weight distribution increases the chance that the stretching speed and the stretching speed will cancel each other out.

なぜならば、このようなポリマーは広範なりラクゼーシ
ョン・スペクトルを有するからである。
This is because such polymers have a broad relaxation spectrum.

部のポリマーは常にノン形態をとる。The polymer in the part always takes a non-form.

急冷することにより、延伸量において得られたシンカパ
ブ形態が応力下で凍結され、該延伸量は高Eモンユラス
および高引張強度を有するフィルムまた(」フィラメン
トとして形成される。
By quenching, the resulting sinker-pab morphology in the stretched volume is frozen under stress, and the stretched volume is formed as a film or filament with high E-monulus and high tensile strength.

本発明は、特にコポリオレフィン、例えば、幾つかのホ
モポリマー、コポリマーまたは2つ以上のコポリマーに
適用できる。
The invention is particularly applicable to copolyolefins, such as several homopolymers, copolymers or copolymers of two or more.

単純な分子構造であるため、プラスデックは好ましくは
400,000〜I 、500,000g1モル、好ま
しくは500,000〜1.200 000g1モル、
さらに好ましくは800 000〜1ooo、oooの
Mwを有するポリエチレンから構成される。
Due to its simple molecular structure, Plusdec preferably has a molecular weight of 400,000 to I, 500,000 g per mol, preferably 500,000 to 1.200 000 g per mol,
More preferably, it is made of polyethylene having a Mw of 800,000 to 1ooo, ooo.

本明細書中のポリエチレンとして、3つ以上の炭素原子
を有するアルケン−Iを多くとも3重量%含有するエヂ
レンのコポリマーが挙げられる。
Polyethylene herein includes copolymers of ethylene containing at most 3% by weight of alkenes-I having 3 or more carbon atoms.

400.000〜1,000,000g1モルのMwを
有するポリエチレンの場合、延伸温度は好ましくは13
0〜160℃、特に好ましくは140〜160℃である
。その他のポリマーに対しては、これらの限界は変更で
きる。400,000−1,000,000g1モルの
Mwを有するポリエヂレンの場合、延伸速度は好ましく
は0.1〜10sec=、さらに好ましくは0 、5−
55ec−’である。
For polyethylene with Mw of 400.000 to 1,000,000 g 1 mol, the stretching temperature is preferably 13
The temperature is 0 to 160°C, particularly preferably 140 to 160°C. For other polymers, these limits can vary. In the case of polyethylene having a Mw of 400,000-1,000,000 g/mol, the stretching speed is preferably 0.1-10 sec=, more preferably 0,5-
55ec-'.

本発明は、また、押出機と、少なくとも供給ロール、引
取ロールおよびその間にある加熱炉から構成される下流
延伸装置とからなる本発明を実施するための装置に関す
る。該装置は、押出機と供給ロールの間に、押出物をプ
ラスチックの押出し温度と溶融温度の間の温度に冷却す
るための冷却装置が配置され、1つ以上の供給ロールが
加熱ロールであり、延伸体を急冷するために加熱炉と弓
取ロールの間に手段を設けたことにより特徴ずけられる
The invention also relates to an apparatus for carrying out the invention, consisting of an extruder and a downstream drawing device consisting of at least a feed roll, a take-off roll and a heating furnace therebetween. The apparatus includes a cooling device disposed between the extruder and the feed roll for cooling the extrudate to a temperature between the extrusion temperature and the melting temperature of the plastic, one or more of the feed rolls being a heating roll; It is characterized by the provision of means between the heating furnace and the Yumitori roll to rapidly cool the stretched body.

上手に設計された装置により、延伸中の押出物の温度の
制御が可能である。押出温度によって、冷却装置内の温
度を制御することにより、もはや押出工程の温度に関係
なく延伸工程を実施できる。
With well designed equipment it is possible to control the temperature of the extrudate during drawing. By controlling the temperature in the cooling device according to the extrusion temperature, the stretching process can no longer be carried out regardless of the temperature of the extrusion process.

冷却装置は液体または気体により制御できる。The cooling device can be controlled by liquid or gas.

以下、実施例により本発明をさらに具体的に説明する。Hereinafter, the present invention will be explained in more detail with reference to Examples.

実施例 そのMw、 Mn(数平均分子量)およびMw/Mw比
並びにその製造者とともに第1表に示したように、多数
のポリエチレン・グレードを試験に用いた。
EXAMPLES A number of polyethylene grades were used in the tests as shown in Table 1 along with their Mw, Mn (number average molecular weight) and Mw/Mw ratios and their manufacturers.

温度+ 4.5°Cで15分間、圧縮成形し、ついで冷
水中で急冷することにより、厚さ0 、5 mmのポリ
エチレン反応体粉末の試料を作製した。該試料から試験
片を切り出し、溶融温度以上、延伸速度5sec−’で
最大延伸し、ついで応力状態下で冷却した。
Samples of polyethylene reactant powder with a thickness of 0.5 mm were prepared by compression molding for 15 minutes at a temperature of +4.5 °C, followed by quenching in cold water. A test piece was cut from the sample, stretched to a maximum temperature above the melting temperature at a stretching speed of 5 sec-', and then cooled under stress.

インストロン引張試験機により、速度1mm/分で長さ
l0cmの試験片について、引張モノユラスを測定した
。ポリエチレン密度0.97に基づいて該試験片の重量
から断面積を計算した。
The tensile monoculus was measured on a test piece with a length of 10 cm at a speed of 1 mm/min using an Instron tensile tester. The cross-sectional area was calculated from the weight of the test piece based on a polyethylene density of 0.97.

第2表は、延伸温度、延伸比および第1表の各ポリエチ
レンについて測定した強度特性を示す。
Table 2 shows the stretching temperature, stretching ratio, and strength properties measured for each polyethylene in Table 1.

第1表および第2表から明らかなように、Mw400.
000未満では、高延伸比でも良好な機械的特性を得る
ことができなかった。Mwl、00o、ooo以上ては
ポリエチレンの処理が困難であるばかりでなく、得られ
た機械的特性はどれも驚く程興味のあるものではなかっ
た。ヒゼックス(Hizex) 2420 Mの引張強
度は僅か0J5GPaであった。
As is clear from Tables 1 and 2, Mw400.
If it was less than 000, good mechanical properties could not be obtained even at a high draw ratio. Not only is it difficult to process polyethylene above Mwl, 00o, ooo, but none of the mechanical properties obtained are surprisingly interesting. The tensile strength of Hizex 2420 M was only 0J5GPa.

第1図は本発明の装置を示す概略図であり、それにより
本発明方法を実施できる。押出機(1)からのフィラメ
ント、テープまたはフィルム形態の押出物は冷却装置(
2)に供給され、そこで押出物はその溶融温度以下に冷
却される。冷却ロールからの冷却され未配向の押出物は
供給ロール部分に供給され、該供給ロールは、例えば、
供給ロール(4)のみが加熱ロールであり、プラスチッ
クの融点より5〜lO℃下に加熱され、ついで引取ロー
ル (5)により炉(6)を通して連続的に引き抜かれ
る。該炉は押出物を130〜160℃の温度に加熱する
。引取ロール(5)はロール(4)よりも周速か速いた
め、炉内で延伸が生じる。ロール(3)および(4)は
周速か同じである。冷却装置(2)および加熱された供
給ロール(4)により、延伸される押出物を炉内で良好
な温度に制御される。加熱炉(6)と引取ロール(5)
、(7)の間には、応ツノ状態下で延伸体を急冷するた
めの手段が概略的に示されている。
FIG. 1 is a schematic representation of an apparatus according to the invention, with which the method according to the invention can be carried out. The extrudate in filament, tape or film form from the extruder (1) is fed to a cooling device (
2) where the extrudate is cooled below its melting temperature. The cooled, unoriented extrudate from the chill roll is fed to a feed roll section, which feed roll has e.g.
The supply roll (4) is the only heated roll and is heated to 5-10° C. below the melting point of the plastic and is then continuously withdrawn through the furnace (6) by a take-off roll (5). The furnace heats the extrudate to a temperature of 130-160°C. Since the take-up roll (5) has a faster circumferential speed than the roll (4), stretching occurs in the furnace. Rolls (3) and (4) have the same circumferential speed. A cooling device (2) and a heated feed roll (4) control the extrudate to be drawn at a good temperature in the furnace. Heating furnace (6) and take-up roll (5)
, (7) schematically shows means for rapidly cooling the stretched body under conditions of stress.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図は本発明の装置を示す概略図である。 図面中の主な符号はつぎのちのを意味する。 1 押出機、2・・冷却装置、4・供給ロール、5・引
取ロール、6 ・加熱炉。
FIG. 1 is a schematic diagram showing the apparatus of the invention. The main symbols in the drawings have the following meanings. 1. Extruder, 2. Cooling device, 4. Supply roll, 5. Take-up roll, 6. Heating furnace.

Claims (10)

【特許請求の範囲】[Claims] (1)比較的高い重量平均分子量(Mw)を有する溶融
体のプラスチックを連続品に変換し、この連続品を未配
向プラスチックの溶融温度(Tm)と、より高温度(T
c)の間の温度で延伸し、延伸速度が、通常の条件下で
の鎖状分子のリラクゼーションの速度より速い速度(V
e)と、それより高いが、溶融体が通常の条件下で弾性
挙動を示し始める程は速くない速度の間にあって、応力
を加えながら延伸された製品を連続体に急冷することを
特徴とするシシカバブ形態を有するプラスチック連続体
の製造方法。
(1) Converting a melt plastic with a relatively high weight-average molecular weight (Mw) into a continuous product, which has a melting temperature (Tm) of the unoriented plastic and a higher temperature (Tm).
c) at a temperature between
characterized in that the drawn product is quenched into a continuum under stress at a rate between e) and higher, but not so high that the melt begins to exhibit elastic behavior under normal conditions. A method for producing a plastic continuum having a shish kebab shape.
(2)プラスチックが400,000〜 1,500,000g/モルのMwを有するポリエチレ
ンである請求項(1)記載の方法。
(2) The method of claim 1, wherein the plastic is polyethylene having a Mw of 400,000 to 1,500,000 g/mol.
(3)プラスチックが500,000〜 1,200,000g/モルのMwを有するポリエチレ
ンである請求項(1)記載の方法。
(3) The method of claim 1, wherein the plastic is polyethylene having a Mw of 500,000 to 1,200,000 g/mol.
(4)プラスチックが800,000〜 1,000,000g/モルのMwを有するポリエチレ
ンである請求項(1)記載の方法。
(4) The method according to claim 1, wherein the plastic is polyethylene having a Mw of 800,000 to 1,000,000 g/mol.
(5)130℃〜160℃の温度で延伸を行う請求項(
1)〜(4)いずれか1項記載の方法。
(5) Claim in which the stretching is carried out at a temperature of 130°C to 160°C (
The method according to any one of 1) to (4).
(6)延伸速度が0.1〜10sec^−^1である請
求項(1)〜(5)いずれか1項記載の方法。
(6) The method according to any one of claims (1) to (5), wherein the stretching speed is 0.1 to 10 seconds^-^1.
(7)延伸速度が0.5〜5sec^−^1である請求
項(1)〜(6)いずれか1項記載の方法。
(7) The method according to any one of claims (1) to (6), wherein the stretching speed is 0.5 to 5 seconds^-^1.
(8)押出機と、少なくとも供給ロール、引取ロールお
よびその間にある加熱炉から構成される下流延伸装置と
からなり、押出機と1つ以上の供給ロールの間に冷却装
置が配置され、片方の供給ロールが加熱ロールであり、
急冷するために加熱炉と引取ロールの間に手段を設けた
ことを特徴とする請求項(1)〜(7)いずれか1項記
載の装置。
(8) Consisting of an extruder and a downstream stretching device consisting of at least a supply roll, a take-up roll, and a heating furnace disposed therebetween, with a cooling device disposed between the extruder and one or more supply rolls, and one of the the supply roll is a heating roll;
8. The apparatus according to claim 1, further comprising means for rapid cooling between the heating furnace and the take-up roll.
(9)図面に記載および/または説明した方法および装
置。
(9) The method and apparatus described and/or illustrated in the drawings.
(10)請求項(1)〜(9)いずれか1項により製造
したプラスチック連続体。
(10) A plastic continuous body produced according to any one of claims (1) to (9).
JP1142019A 1988-06-03 1989-06-02 Method and device for manufacturing plastic continuum Expired - Lifetime JP2675140B2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
NL8801426A NL8801426A (en) 1988-06-03 1988-06-03 METHOD AND APPARATUS FOR MANUFACTURING ENDLESS ARTICLES
NL8801426 1988-06-03

Publications (2)

Publication Number Publication Date
JPH0250817A true JPH0250817A (en) 1990-02-20
JP2675140B2 JP2675140B2 (en) 1997-11-12

Family

ID=19852399

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1142019A Expired - Lifetime JP2675140B2 (en) 1988-06-03 1989-06-02 Method and device for manufacturing plastic continuum

Country Status (8)

Country Link
US (1) US5080849A (en)
EP (1) EP0344860B1 (en)
JP (1) JP2675140B2 (en)
KR (1) KR920007729B1 (en)
AT (1) ATE110127T1 (en)
CA (1) CA1317724C (en)
DE (1) DE68917527T2 (en)
NL (1) NL8801426A (en)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB9027699D0 (en) * 1990-12-20 1991-02-13 Univ Toronto Process for the continuous production of high modulus articles from polyethylene
FI93865C (en) * 1992-05-29 1995-06-12 Borealis Holding As Melt-spun strong polyethylene fiber
BE1007045A3 (en) * 1993-06-04 1995-02-28 Solvay PROCESS FOR THE DIRECT AND CONTINUOUS EXTRUSION OF BIORIENTED TUBULAR STRUCTURES IN CRYSTALLIZABLE POLYMERS.
US6391411B1 (en) 1999-06-03 2002-05-21 Printpack Illinois, Inc. Machine direction oriented high molecular weight, high density polyethylene films with enhanced water vapor transmission properties
WO2008118643A1 (en) * 2007-03-27 2008-10-02 Dow Global Technologies Inc. Low relative crystallinity die drawing process for a cavitated filled oriented polymer composition
CN109440215B (en) * 2018-11-28 2021-02-09 上海化工研究院有限公司 Preparation method of high-performance polyethylene fiber

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1568964A (en) * 1975-11-05 1980-06-11 Nat Res Dev Oriented polymer materials
GB8333032D0 (en) * 1983-12-10 1984-01-18 Bp Chem Int Ltd Orientated polyolefins
NL8502298A (en) * 1985-08-21 1987-03-16 Stamicarbon PROCESS FOR MANUFACTURING HIGH TENSILE STRENGTH AND MODULUS POLYETHYLENE ARTICLES.

Also Published As

Publication number Publication date
CA1317724C (en) 1993-05-18
KR920007729B1 (en) 1992-09-16
EP0344860A1 (en) 1989-12-06
US5080849A (en) 1992-01-14
DE68917527T2 (en) 1995-05-11
JP2675140B2 (en) 1997-11-12
KR900000177A (en) 1990-01-30
ATE110127T1 (en) 1994-09-15
NL8801426A (en) 1990-01-02
EP0344860B1 (en) 1994-08-17
DE68917527D1 (en) 1994-09-22

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